← Back to catalogue

Ace

FDA UDI

Class I (US FDA UDI)

by Ace Surgical Supply Co., Inc.

Identity

Trade Name
ACE FDA UDI
Generic Name
Dental dressing forceps, reusable FDA UDI
Device Name
SPATULA CEMENT STANDARD 7-1/4" 18.5CM FDA UDI
Model / Reference
1118039 FDA UDI
Description
SPATULA CEMENT STANDARD 7-1/4" 18.5CM FDA UDI

Identifiers

Catalog Number
1118039 FDA UDI
Primary DI / UDI-DI
00614950029990 FDA UDI
FDA Product Code
EMH FDA UDI
GMDN Term
Dental dressing forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental dressing forceps, reusable

Ace by Ace Surgical Supply Co., Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental dressing forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 7620942d-8fda-4845-831d-74166fd21324 35 fields · synced Jun 6, 2026